Canonical Allele Identifier: CA1423669395

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179230095A= , CM000665.2:g.179230095A=	GRCh38
NC_000003.11:g.178947883A= , CM000665.1:g.178947883A=	GRCh37
NC_000003.10:g.180430577A=	NCBI36
NG_012113.2:g.86573A= , LRG_310:g.86573A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.2758A= MANE Select	ENSP00000263967.3:p.Asn920=
ENST00000462255.2:n.1781A=
ENST00000643187.1:c.2758A=	ENSP00000493507.1:p.Asn920=
ENST00000674534.1:n.3666A=
ENST00000674622.1:c.1179A=	ENSP00000502417.1:n.1179A=
ENST00000675467.1:n.5565A=
ENST00000675786.1:c.*1325A=	ENSP00000502323.1:n.*1325A=
ENST00000675796.1:n.2653A=
ENST00000263967.3:c.2758A=	ENSP00000263967.3:p.Asn920=
NM_006218.2:c.2758A= , LRG_310t1:c.2758A=	NP_006209.2:p.Asn920=
XM_006713658.2:c.2758A=	XP_006713721.1:p.Asn920=
XM_011512894.1:c.2758A=	XP_011511196.1:p.Asn920=
NM_006218.3:c.2758A=	NP_006209.2:p.Asn920=
XM_006713658.4:c.2758A=	XP_006713721.1:p.Asn920=
XM_011512894.2:c.2758A=	XP_011511196.1:p.Asn920=
NM_006218.4:c.2758A= MANE Select	NP_006209.2:p.Asn920=